US5646106A - Cold pearlizing concentrates - Google Patents

Cold pearlizing concentrates Download PDF

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Publication number
US5646106A
US5646106A US08/367,495 US36749594A US5646106A US 5646106 A US5646106 A US 5646106A US 36749594 A US36749594 A US 36749594A US 5646106 A US5646106 A US 5646106A
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sub
betaine
weight percent
concentrate
emulsifier
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Pu Chen
Siew Fang Yoong
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Rhodia Operations SAS
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Rhone Poulenc Specialty Chemicals Asia Pacific Pte Ltd
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Assigned to RHONE-POULENC SPECIALTY CHEMICALS ASIA PACIFIC PTE LTD. reassignment RHONE-POULENC SPECIALTY CHEMICALS ASIA PACIFIC PTE LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: YOONG, SIEW F., CHEN, PU
Priority to PCT/US1996/000252 priority patent/WO1996021711A2/fr
Priority to AU48964/96A priority patent/AU706498B2/en
Priority to JP52177096A priority patent/JP3717935B2/ja
Priority to CN96191688A priority patent/CN1172427A/zh
Assigned to RHONE-POULENC INC. reassignment RHONE-POULENC INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: RHONE-POULENC SPECIALTY CHEMICALS ASIA PACIFIC PTE LTD.,(A SINGAPORE CORPORATION)
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Assigned to RHODIA INC. reassignment RHODIA INC. INVALID RECORDING. SEE RECORDING AT REEL 010404, FRAME 0268. Assignors: RHONE-POULENC INC.
Priority to JP2003066331A priority patent/JP3790223B2/ja
Assigned to RHODIA OPERATIONS reassignment RHODIA OPERATIONS ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: RHODIA INC.
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    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0089Pearlescent compositions; Opacifying agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • A61K8/442Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof substituted by amido group(s)
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/46Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • A61K8/463Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfuric acid derivatives, e.g. sodium lauryl sulfate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/10Washing or bathing preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/02Preparations for cleaning the hair
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/88Ampholytes; Electroneutral compounds
    • C11D1/94Mixtures with anionic, cationic or non-ionic compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59Mixtures
    • A61K2800/596Mixtures of surface active compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/29Sulfates of polyoxyalkylene ethers
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/52Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
    • C11D1/523Carboxylic alkylolamides, or dialkylolamides, or hydroxycarboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 contain one hydroxy group per alkyl group
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/667Neutral esters, e.g. sorbitan esters
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/88Ampholytes; Electroneutral compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/88Ampholytes; Electroneutral compounds
    • C11D1/90Betaines
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/88Ampholytes; Electroneutral compounds
    • C11D1/92Sulfobetaines ; Sulfitobetaines

Definitions

  • the present invention relates generally to hair and skin compositions such as soaps and shampoos for washing the skin and conditioning the hair. More particularly, the present invention relates to cold pearlescent concentrates used in said soaps and shampoos which impart an iridescent sheen or glow to these compositions.
  • Hair conditioning shampoos and cosmetic soaps are well known in the art and have been described extensively in both the patent and non-patent journal literature.
  • Cationic surfactants such as quaternary ammonium salts and anionic surfactants such as fatty alcohol sulfates and alkyl benzene sulfonates have been employed in hair rinses, soaps and shampoos as conditioning agents together with other water insoluble conditioning compounds such as silicones, waxes, grease and oils.
  • Shampoos and soaps have always been produced in a variety of different forms such as solid bars, gels, creams and liquids.
  • Pearlescent shampoos are comprised of a number of ingredients such as stabilizing agents, pearlescent agents, conditioners, emulsifiers and hydrating agents. Pearlescent agents produce a shiny glow-like look to the compositions by the incorporation of substances which, after cooling, precipitate in the form of fine crystals resembling mother of pearl and which remain dispersed in the preparation.
  • Known pearlizing agents include the mono- ⁇ and diesters of glycol and glycerol with C 6-C 22 fatty acids.
  • most pearlescent agents of the prior art if used by themselves, have to be heated above their melting points for incorporation into a final formulation. The heating step and the conditions after the heating, e.g., the mixing, storage and/or cooling stages are difficult to control and thus the pearlescence condition is ofttimes not optimized, i.e., less than ideal.
  • Cold pearlescent concentrates i.e., those that can be subsequently formulated at room temperature, are known to offer a more consistent final pearlescent product.
  • the room temperature blending not only saves energy, but also eliminates many inconsistencies that occur with high temperature mixing.
  • Cocodiethanolamide has been used to prepare these cold pearlescent concentrates since it is liquid at room temperature and thus does not require a melting step to prepare the formulations; however, studies have raised concern that the diethanolamine, often present as a by-product of the cocodiethanolamide production, may form potentially carcinogenic nitrosamines. Thus, the use of cocodiethanolamide in pearlescent personal hair care and skin products such as cosmetics, facial soaps and shampoos has been questioned from a health standpoint.
  • U.S. Pat. No. and 5,290,482 to Marschner et al. discloses surfactant compositions comprising betaine/cocoamide complexes for use in shampoo and skin cleansing products.
  • the complexes are combined with a cationic, non-ionic, amphoteric or anionic surfactant to provide improved lather and conditioning characteristics.
  • Cocodiethanolamide is widely used in these shampoo compositions. See U.S. Pat. No. 4,534,877 to Russell et. al.
  • Cocoamidopropyl betaine is also a common shampoo ingredient often used as a conditioner or foam enhancer to increase the richness of the lather. See U.S. Pat. No. 4,490,355 to Desai.
  • U.S. Pat. No. 5,217,711 to DeOliveira et. al. disclose a hair treatment system consisting of a shampoo comprising, among other things, a pearlizing agent consisting of glycol distearate and a cocodiethanolamide.
  • U.S. Pat. No. 5,019,376 to Vick teaches pearlescent "crystals" in a shampoo formulation formed by the reaction between a fatty acid and a fatty monoalcohol.
  • U.S. Pat. No. 4,959,206 to Noguera et. al. teaches distearate of ethylene glycol and laurylsulfosuccinate as pearlescent agents but again, cocodiethanolamide is a necessary pearlescent stabilizer.
  • U.S. Pat. No. 4,938,953 to Pena discloses conditioning shampoos comprised of a fatty acid sulfate or a fatty alcohol ether sulfate, cocoamidopropyl betaine and cocoamidodiethanolamine. This composition also utilizes sodium lauryl sulfate as a stabilizing agent.
  • U.S. Pat. No. 5,271,930 to Walele et. al. discloses the use of novel benzoic acid esters of polyalkoxylated block co-polymers as pearlescent agents in hair and skin care compositions.
  • Pearlizing agents conventionally can contain ethylene glycol monostearate, ethylene glycol distearate, guanine bismuth oxychloride on mica and mixtures thereof.
  • U.S. Pat. No. 4,654,207 to Preston teaches a pearlescent shampoo wherein the pearlescing agent is a fatty acid ester, such as myristyl myristate or cetyl myristate, which is added to the shampoo base from a substantially anhydrous solubilizing agent such as a surfactant.
  • a substantially anhydrous solubilizing agent such as a surfactant.
  • a number of other prior art patents such as U.S. Pat. No. 4,608,392 to Jaquet et. al. describe the use of fatty alcohols and fatty acid quaternary ammonium compounds in the pearlescent blends.
  • Pat. No. 5,019,376 to Vick et. al. also teaches the use of a quaternary ammonium compounds such as stearyl dimethyl benzyl ammonium chloride together with a C 12 -C 6 fatty acid and cetyl alcohol.
  • U.S. Pat. No. 5,213,792 to Grundemen discloses hair conditioning compositions containing a pearlescent agent comprised of glycerin, a monolauric acid ester, a C 10 -C 18 fatty alcohol, a quaternary ammonium compound, water and any one of a number of dyes, antioxidants and the like. All of these compositions also use cocodiethanolamide in one form or another for pearlescence or some other related function.
  • U.S. Pat. No. 4,777,038 to Scheuffgen discloses a free flowing pearlescent concentrate which allegedly remains stable without the sedimentation of the pearlescent crystals during storage.
  • the composition is comprised of at least one mono- and diester of ethylene glycol or propylene glycol, a fatty acid mono-ethanolamine, ethylene glycol distearate, coconut oil and fatty alcohol.
  • the sheen is provided by the appearance of fine, pearlescent crystals.
  • a free flowing pearlescent concentrate comprising a C 12 -C 18 coconut oil fatty acid monoethanolamide, a C 16 -C 22 fatty alkyl ester, and at least one ethylene or propylene glycol ester or diester.
  • These pearlescent agents act as emulsifiers which provide free flowing dispersions that allegedly combine high brilliance and stability with other cationic surfactant components.
  • U.S. Pat. No. 5,198,209 to Zhou et. al. discloses a conditioning shampoo comprising a mixture of anionic, cationic and nonionic surfactants and suggests the use of ethylene glycol stearate among others as a pearlescent agent.
  • U.S. Pat. No. 5,252,325 to Bires et. al. teaches a polyvinyl-pyrrolidone stabilized silicone shampoos together with a cationic surfactant and ethylene glycol distearate as a suggested pearlescent agent.
  • the present invention comprises a novel cold pearlescent concentrate for use in shampoo, lipstick, skin creams and lotions and the like and a method for its preparation.
  • the pearlizing concentrate agent is a unique formulation of ingredients comprised of an emulsifier, a zwitterionic, a nonionic alcohol ethoxylate, and an anionic alkyl or alkyl ether sulfate which when processed with other surfactants under conditions known in the art, impart a brilliant sheen when incorporated into shampoo and soap products.
  • a stable, free flowing cold pearlescent concentrate is prepared using i) a suspending agent emulsifier, preferably a glycol stearate; ii) a zwitterionic co-emulsifier; iii) a nonionic alcohol ethoxylate; and iv) an anionic alkyl or alkyl ether sulfate to obviate the use of cocodiethanolamide which is found in the cold compositions of the prior art.
  • a suspending agent emulsifier preferably a glycol stearate
  • ii) a zwitterionic co-emulsifier iii) a nonionic alcohol ethoxylate
  • an anionic alkyl or alkyl ether sulfate to obviate the use of cocodiethanolamide which is found in the cold compositions of the prior art.
  • the emulsifier comprises from about 15 to about 25 weight percent of the present concentrate, and preferably from about 18 to 22% based on the total weight of the concentrate.
  • the emulsifier is preferably selected from the group consisting of hydroxy stearate, polyethylene glycol mono- and distearates, ethylene glycol mono- and distearates, stearic monoethanolamide, stearic monoethanolamide stearate and mixtures thereof.
  • the most preferred emulsifier is ethylene glycol monostearate (C 17 H 35 COO(CH 2 ) 2 OH).
  • a second component of the pearlizing concentrate is a nonionic surfactant.
  • This surfactant which functions as an emulsion stabilizer in the formulation, is preferably an alcohol ethoxylate, of the formula
  • R is a C 8 -C 22 alkyl, preferably C 10 -C 18 ; and n is 1-40, preferably 3-20.
  • the most preferred nonionic is a lauryl alcohol ethoxylate such as Rhodasurf® LA-7, a C 12 alkyl (7) ethoxylated alcohol sold by Rhone-Poulenc Inc.
  • the nonionic surfactant is incorporated in the cold pearlizing concentrate in an amount of from approximately 1.0 weight percent to about 20.0 weight percent; preferably in an amount of from about 5.0 to about 10.0 weight percent; and most preferably about 7 to 10 weight percent based on the total weight of the concentrate.
  • An artionic surfactant preferably an alkyl sulfate or alkyl ether sulfate of the following formulae:
  • R 1 is a C 8 -C 20 alkyl or C 8 -C 20 alkyl C 6 -C 122 aryl group, preferably C 8 -C 11 alkyl; n is 1-40, preferably 3-20; and M is a counterion selected from the group consisting of sodium, calcium, magnesium, ammonium and triethanolamine, is the third component of the concentrate and is necessary both as a surfactant and a wetting agent in the cold pearlizing concentrates of this invention.
  • the anionic surfactant is a sodium laureth sulfate, e.g. sodium lauryl-(3EO) sulfate, such as those of the RHODAPEX® series sold by Rhone-Poulenc Inc.
  • the anionic is present from about 1 to about 20 weight percent, preferably from about 4 to about 18 weight percent; most preferably from about 10 to about 12 weight percent based on the total concentrate.
  • Ethylene glycol stearate together with sodium laureth sulfate provide excellent stabilizing qualities.
  • a zwitterionic surfactant comprises the fourth component of the present invention.
  • Zwitterionic surfactants are those in which the positive and negative groups are equally ionized.
  • zwitterionic surfactants known as the betaines and their derivatives are incorporated to provide an enhanced pearlizing effect.
  • Betaines and amidobetaines are compounds of the general structures: ##STR1## respectively wherein R 2 is C 8 -C 22 alkyl or alkeny; R 3 is H or C 1 -C 4 alkyl; and R 4 is H or C 1 -C- 4 alkyl.
  • the more preferred betaines useful herein include the high alkyl betaines such as cocodimethyl carboxymethyl betaine, lauryl dimethyl carboxymethyl betaine, lauryl dimethyl alpha-carboxy-ethyl betaine, cetyl dimethyl carboxymethyl betaine, lauryl bis-(2-hydroxy-ethyl)carboxy methyl betaine, stearyl bis-(2-hydroxy-propyl)carboxymethyl betaine, oleyl dimethyl gamma-carboxypropyl betaine, and lauryl bis-(2-hydroxypropyl)alpha-carboxyethyl betaine.
  • high alkyl betaines such as cocodimethyl carboxymethyl betaine, lauryl dimethyl carboxymethyl betaine, lauryl dimethyl alpha-carboxy-ethyl betaine, cetyl dimethyl carboxymethyl betaine, lauryl bis-(2-hydroxy-ethyl)carboxy methyl betaine, stearyl bis-(2-hydroxy-
  • the sulfobetaines are also preferred and may be represented by cocodimethyl sulfopropyl betaine, stearyldimethyl sulfopropyl betaine, lauryl dimethyl sulfoethyl betaine, and lauryl bis-(2-hydroxy-ethyl)sulfopropyl betaine.
  • a particularly preferred composition utilizes cocoamidopropyl betaine.
  • the zwitterionic can be present from approximately 1.0 weight percent to about 10 weight percent based on the total weight of the pearlizing concentrate. Preferably, the zwitterionic will comprise from about 2.0 to about 7.0 weight percent of the composition and most preferably from about 3.0 to about 5.0 weight percent of the pearlizing concentrate.
  • Water preferably deionized, is then added in an amount from about 25 weight percent to about 82 weight percent, preferably from about 48 to about 65 weight percent based on the total weight of the concentrate.
  • the formulated shampoo and soap systems utilizing the cold pearlizing concentrate of the present invention can contain a variety of non-essential optional components suitable for rendering such compositions more acceptable.
  • non-essential optional components suitable for rendering such compositions more acceptable.
  • conventional optional ingredients are well known to those skilled in the art, e.g., preservatives such as benzyl alcohol, methyl paraben, propyl paraben and imidazolidinyl urea; cationic surfactants such as cetyl trimethyl ammonium chloride, lauryl trimethyl ammonium chloride, tricetyl methyl ammonium chloride, stearyldimethyl benzyl ammonium chloride, and di(partially hydrogenated tallow) dimethylammonium chloride; thickeners and viscosity modifiers such as block polymers of ethylene oxide and propylene oxide, e.g.
  • Antarox F-88 (Rhone-Poulenc Inc.), sodium chloride, sodium sulfate, polyvinyl alcohol, and ethyl alcohol; pH adjusting agents such as citric acid, succinic acid, phosphoric acid, sodium hydroxide, sodium carbonate; perfumes; dyes; and sequestering agents such as disodium ethylenediamine tetra-acetate.
  • pH adjusting agents such as citric acid, succinic acid, phosphoric acid, sodium hydroxide, sodium carbonate
  • perfumes dyes
  • sequestering agents such as disodium ethylenediamine tetra-acetate.
  • Such agents generally are used individually at levels of from about 0.01% to about 10%, preferably from 0.5% to about 5.0% by weight of the composition.
  • the pH of the present compositions is not critical and may be in the range of from about 5 to about 9.
  • the pH can be adjusted using a buffer such as citric acid.
  • the order of addition to the mixing tank of the individual components of the concentrate is not critical nor is the reasonably elevated temperature; however, preferably the water, emulsifier and anionic surfactant are intimately blended at from about 60° to 80° C., more preferably from about 70° to 75° C. with high agitation until the emulsifier is solubilized.
  • the nonionic surfactant and zwitterionic are then blended into the mix.
  • the concentrate is then stored at a temperature of from about 35° C. to about 60° C., preferably from about 45° C. to about 55° C. for at least one day and preferably two (2) days in order to fully develop its pearlescent characteristics.
  • the shampoos and soaps of the present invention can be made by merely mixing the materials together with the concentrate at room temperature.
  • the cold pearlizing concentrate of the present invention may be specifically formulated into a number of different blended soap products.
  • the pearlizing concentrate not only imparts a high luster pearlescence and sheen to the products, but also contributes emollient and moisturizing qualities to the skin. It provides superior shampoo, bath and shower soap systems and markedly improves wet comb-out of the hair.
  • compositions of the present invention are for illustrative purposes only, and it is realized that minor changes and variations may be made with respect to these compositions that are not shown below. Such changes that do not materially alter the compositions formulation or function are still considered to fall within the spirit and scope of the invention as recited by the claims that follow.
  • the ethylene glycol monostearate is mixed with water and the sodium lauryl sulfate at 70° to 75° C. with high speed agitation.
  • the laureth(7EO) alcohol and the cocoamidopropyl betaine are added into the mixture with stirring and kept at 50° C. for one to two days in order to develop the pearlescence fully. The maintenance of the emulsion at this temperature for this period of time is important for the full development of the pearlescence.
  • the pearlescence concentrate produced is an iridescent or shiny white to off-white viscous liquid with a pH from about 6.5-7.5 and realizes excellent dispersibility in water.
  • compositions of this invention require no heating for blending and are readily compatible with most anionic-based liquid hand cleaner, shampoo, bubble bath and cosmetic systems to form attractive high-performance products.
  • the water is charged into a mixing vessel and the active ingredients are slowly mixed at room temperature until the mixture becomes uniform in appearance and texture.
  • Citric acid 50%) is then added in an amount sufficient to adjust the pH to 6.0.
  • the shampoo is then fragranced with a suitable perfume as desired and colored with an appropriate FD & C. dye.
  • the hand soap provides excellent lather and cleaning and leaves the hands soft.
  • Example II The ingredients are easily blended as in Example II. These pearlescent specialty bath and shower formulations contribute to a luxurious, smooth feel and they help to keep the skin soft and supple.
  • a body shampoo (6) and a shampoo/bubble bath (7) are prepared as in the body shampoo (4) and shampoo/bubble bath (5) of Example III with the use of Formulation C concentrate in lieu of Formulation B.
  • the pearlescent liquid products are prepared easily at room temperature and the Formulation C. concentrate provides enhanced viscosity building, foam stability and lather enrichment properties.

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US08/367,495 1994-12-30 1994-12-30 Cold pearlizing concentrates Expired - Lifetime US5646106A (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
US08/367,495 US5646106A (en) 1994-12-30 1994-12-30 Cold pearlizing concentrates
PCT/US1996/000252 WO1996021711A2 (fr) 1994-12-30 1996-01-02 Concentres nacres prepares a froid
AU48964/96A AU706498B2 (en) 1994-12-30 1996-01-02 Cold pearlizing concentrates
JP52177096A JP3717935B2 (ja) 1994-12-30 1996-01-02 常温真珠光沢化濃縮物
CN96191688A CN1172427A (zh) 1994-12-30 1996-01-02 冷珠光化浓缩物
JP2003066331A JP3790223B2 (ja) 1994-12-30 2003-03-12 常温真珠光沢化濃縮物の製造方法

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US08/367,495 US5646106A (en) 1994-12-30 1994-12-30 Cold pearlizing concentrates

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CN (1) CN1172427A (fr)
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WO2000010510A1 (fr) * 1998-08-20 2000-03-02 Cognis Deutschland Gmbh Utilisation de dispersions aqueuses de cire comme epaississant
US6165955A (en) * 1997-03-06 2000-12-26 Rhodia Inc. Mild cold pearlizing concentrates
ES2185497A1 (es) * 2001-07-30 2003-04-16 Kao Corp Sa Composiciones nacarantes acuosas concentradas.
US20040105831A1 (en) * 2002-08-13 2004-06-03 Seren Frantz Compositions having a pearl blend appearance additive, personal care products made therefrom
US20050158270A1 (en) * 2004-01-15 2005-07-21 Seren Frantz Pearlizer concentrate and its use in personal care compositions
WO2006027213A1 (fr) * 2004-09-09 2006-03-16 Unilever Plc Methode de preparation d'une composition d'hygiene personnelle a partir d'une composition de base et methode de preparation de ladite composition de base
US20070173180A1 (en) * 2003-10-17 2007-07-26 Swei Gwo S Antiloading compositions and methods of selecting same
US20100038585A1 (en) * 2007-03-12 2010-02-18 Kao Corporation Pearlescent composition
WO2015059711A1 (fr) * 2013-10-25 2015-04-30 Galaxy Surfactants Ltd. Concentré nacré dispersible à froid durable
US9138429B2 (en) 2011-06-23 2015-09-22 The Procter & Gamble Company Process of forming crystals for use in a personal care composition
WO2016034635A1 (fr) * 2014-09-03 2016-03-10 Henkel Ag & Co. Kgaa Composition détergente liquide à éclat perlé
US9474916B2 (en) 2013-08-08 2016-10-25 Evonik Degussa Gmbh Carbamates from glycerine carbonate for pearlization

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DE19646882C2 (de) 1996-11-13 1998-09-24 Henkel Kgaa Wäßrige Perlglanzkonzentrate
KR100443400B1 (ko) * 1997-05-22 2004-10-08 주식회사 엘지생활건강 고형상의 주방용세제 조성물
DE10162024A1 (de) 2001-12-18 2003-07-03 Cognis Deutschland Gmbh Hochkonzentriert fließfähige Perlglanzkonzentrate
CN101631531B (zh) * 2007-03-12 2012-03-28 花王株式会社 珠光组合物
JP5311875B2 (ja) * 2007-06-13 2013-10-09 花王株式会社 パール光沢組成物
JP2008013581A (ja) * 2007-10-03 2008-01-24 Kao Corp パール光沢組成物
WO2016034633A1 (fr) * 2014-09-03 2016-03-10 Henkel Ag & Co. Kgaa Composition détergente liquide à lustre nacré
KR20210137117A (ko) 2019-03-13 2021-11-17 바스프 에스이 왁스 분산물을 위한 안정화제 농축물
ES2971937T3 (es) 2019-09-18 2024-06-10 Basf Se Concentrados estabilizadores para dispersiones de cera

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US4490355A (en) * 1983-03-14 1984-12-25 Miranol Chemical Company, Inc. Betaine based cosmetic formulations
US4608392A (en) * 1983-08-30 1986-08-26 Societe Anonyme Dite: L'oreal Method for producing a non greasy protective and emollient film on the skin
US4654207A (en) * 1985-03-13 1987-03-31 Helene Curtis Industries, Inc. Pearlescent shampoo and method for preparation of same
US4777038A (en) * 1985-05-28 1988-10-11 Henkel Kommanditgesellschaft Auf Aktien Free-flowing pearlescent concentrate
US4728457A (en) * 1986-08-25 1988-03-01 The Proctor & Gamble Company Process for making a silicone-containing shampoo
US5017305A (en) * 1986-11-28 1991-05-21 Henkel Kommanditgesellschaft Auf Aktien Free-flowing pearlescent concentrate
US4948528A (en) * 1986-11-28 1990-08-14 Henkel Kommanditgesellschaft Auf Aktien Free-flowing pearlescent concentrate
US4824594A (en) * 1986-11-28 1989-04-25 Henkel Kommanditgesellschaft Auf Aktien Free-flowing pearlescent concentrate
US4885107A (en) * 1987-05-08 1989-12-05 The Procter & Gamble Company Shampoo compositions
US5151209A (en) * 1987-11-19 1992-09-29 The Procter & Gamble Company Shampoo compositions
US4959206A (en) * 1987-12-28 1990-09-25 Kao Corporation Pearling agent dispersion
US4938953A (en) * 1988-08-09 1990-07-03 The Upjohn Company Self-preserving conditioning shampoo formulation
US5213792A (en) * 1988-11-08 1993-05-25 Wella Aktiengesellschaft Storage-stable pearlescent hair-conditioning compositions
US5019376A (en) * 1989-03-13 1991-05-28 S. C. Johnson & Son, Inc. Sparkling pearlescent personal care compositions
US5152914A (en) * 1989-05-30 1992-10-06 Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. Shampoo composition
US5290248A (en) * 1989-07-24 1994-03-01 Steven F. Bierman Sideport connector for catherization system
US5275755A (en) * 1990-05-18 1994-01-04 L'oreal Washing compositions based on silicone and on fatty alcohols containing ether and/or thioether or sulphoxide groups
US5252325A (en) * 1991-01-08 1993-10-12 Isp Investments Inc. Conditioning hair care compositions
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Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6165955A (en) * 1997-03-06 2000-12-26 Rhodia Inc. Mild cold pearlizing concentrates
WO2000010510A1 (fr) * 1998-08-20 2000-03-02 Cognis Deutschland Gmbh Utilisation de dispersions aqueuses de cire comme epaississant
US6562876B1 (en) 1998-08-20 2003-05-13 Cognis Deutschland Gmbh & Co. Kg Use of aqueous wax dispersions as consistency providers
ES2185497A1 (es) * 2001-07-30 2003-04-16 Kao Corp Sa Composiciones nacarantes acuosas concentradas.
US20040105831A1 (en) * 2002-08-13 2004-06-03 Seren Frantz Compositions having a pearl blend appearance additive, personal care products made therefrom
US20070169420A1 (en) * 2003-10-17 2007-07-26 Saint-Gobain Abrasives, Inc. Antiloading compositions and methods of selecting same
US20090199487A1 (en) * 2003-10-17 2009-08-13 Saint-Gobain Abrasives, Inc. Antiloading compositions and methods of selecting same
US20070173180A1 (en) * 2003-10-17 2007-07-26 Swei Gwo S Antiloading compositions and methods of selecting same
US8337574B2 (en) 2003-10-17 2012-12-25 Saint-Gobain Abrasives, Inc. Antiloading compositions and methods of selecting same
US20050158270A1 (en) * 2004-01-15 2005-07-21 Seren Frantz Pearlizer concentrate and its use in personal care compositions
US20080262101A1 (en) * 2004-09-09 2008-10-23 Maria Teresa Belmar Method to Prepare a Personal Care Composition From a Base Composition and a Method to Prepare the Base Composition
WO2006027213A1 (fr) * 2004-09-09 2006-03-16 Unilever Plc Methode de preparation d'une composition d'hygiene personnelle a partir d'une composition de base et methode de preparation de ladite composition de base
US20100038585A1 (en) * 2007-03-12 2010-02-18 Kao Corporation Pearlescent composition
US8529788B2 (en) 2007-03-12 2013-09-10 Kao Corporation Pearlescent composition
US9138429B2 (en) 2011-06-23 2015-09-22 The Procter & Gamble Company Process of forming crystals for use in a personal care composition
US10117813B2 (en) 2011-06-23 2018-11-06 The Procter And Gamble Company Process of forming crystals for use in a personal care composition
US9474916B2 (en) 2013-08-08 2016-10-25 Evonik Degussa Gmbh Carbamates from glycerine carbonate for pearlization
WO2015059711A1 (fr) * 2013-10-25 2015-04-30 Galaxy Surfactants Ltd. Concentré nacré dispersible à froid durable
WO2016034635A1 (fr) * 2014-09-03 2016-03-10 Henkel Ag & Co. Kgaa Composition détergente liquide à éclat perlé

Also Published As

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WO1996021711A2 (fr) 1996-07-18
AU4896496A (en) 1996-07-31
CN1172427A (zh) 1998-02-04
WO1996021711A3 (fr) 1996-11-14
JP2003246713A (ja) 2003-09-02
JP3717935B2 (ja) 2005-11-16
JP3790223B2 (ja) 2006-06-28
AU706498B2 (en) 1999-06-17
JPH10510541A (ja) 1998-10-13

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